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rs1057518373

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518373(C;C)
Make rs1057518373(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165344766
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057518373
dbSNP (classic)rs1057518373
ClinGenrs1057518373
ebirs1057518373
HLIrs1057518373
Exacrs1057518373
Gnomadrs1057518373
Varsomers1057518373
LitVarrs1057518373
Maprs1057518373
PheGenIrs1057518373
Biobankrs1057518373
1000 genomesrs1057518373
hgdprs1057518373
ensemblrs1057518373
geneviewrs1057518373
scholarrs1057518373
googlers1057518373
pharmgkbrs1057518373
gwascentralrs1057518373
openSNPrs1057518373
23andMers1057518373
23andMe allrs1057518373
SNPshotrs1057518373
SNPdbers1057518373
MSV3drs1057518373
GWAS Ctlgrs1057518373
Max Magnitude0
ClinVar
Risk rs1057518373(C;C)
Alt rs1057518373(C;C)
Reference Rs1057518373(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201276T>C
CLNSRC
CLNACC RCV000413714.1,